A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899874



Internal ID16193830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43209447..43344645hg38UCSC Ensembl
Innerchr19:43713599..43848797hg19UCSC Ensembl
Innerchr19:48405439..48540637hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38135199
hg19135199
hg18135199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579825
Supporting Variants
Samples
Known GenesLOC284344, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer